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About
Background:
Treatments for structural heart and valve disease are quickly changing. But treatment could be improved. Researchers want to gather data from people with this disease. They want to find problems and seek new ways to make treatments better.
Objective:
To find people with structural heart and valve disease with common features to study. To find flaws and patterns in procedures related to this disease. To share findings with other researchers.
Eligibility:
People ages 18 and older who are receiving care from the structural heart and valve program at the participating NHLBI structural heart disease network sites that are part of the study
Design:
Participants will be screened with their consent. This will occur when they give their standard consent for medical care.
Participants will have their data collected in the course of standard medical care. Data include:
Demographic data
Protected health data
Personally identifiable data
Medical records
Medical images. These could include X-rays, CT scans, and MRI scans.
The study could find something that would impact participants care. If this is the case, their doctors will be told.
Participants data may be shared with other researchers.
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Full description
Medical care is evolving rapidly for patients considered for treatment of structural heart and valve disease. Despite technical advances, many shortcomings remain. This research protocol allows researchers to pool medical records and imaging studies to identify problems and seek new solutions.
All patients considered for treatment at participating NHLBI structural heart and valve centers are invited to allow researchers to access their medical records repeatedly, including the results of medical procedures and imaging studies such as catheterization, CT, echocardiography, and MRI. These records, which include patient identity, will be sent to a central NHLBI database and kept confidential. Results will be used in medical publications but patient identity will be hidden.
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Inclusion and exclusion criteria
EXCLUSION CRITERIA:
0 participants in 1 patient group
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Data sourced from clinicaltrials.gov
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